Identity
- Trade Name
- SYSTEM 2450 EUDAMEDFDA UDI
- Generic Name
- Electrosurgical system generator FDA UDI
- Device Name
- Non-orthopedic, Active, Electrosurgical Generator, General purpose, System 2450 EUDAMEDSYSTEM 2450 220 VAC 50/60 Hz Electrosurgical Unit FDA UDISYSTEM 2450 100 VAC 50/60 Hz Electrosurigcal Unit FDA UDI
- Model / Reference
- 60-2450-220 EUDAMEDFDA UDI60-2450-100 EUDAMEDFDA UDI
- Description
- SYSTEM 2450 220 VAC 50/60 Hz Electrosurgical Unit FDA UDISYSTEM 2450 100 VAC 50/60 Hz Electrosurigcal Unit FDA UDI
Identifiers
- Catalog Number
- 60-2450-220 FDA UDI60-2450-100 FDA UDI
- Primary DI / UDI-DI
- 20653405058158 EUDAMEDFDA UDI20653405058141 EUDAMEDFDA UDI
- Basic UDI-DI
- B-20653405058158 EUDAMEDB-20653405058141 EUDAMED
- FDA Product Code
- GEI FDA UDI
- EMDN Code
- Z12010902 ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE EUDAMED
- GMDN Term
- Electrosurgical system generator FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Foot-switch, electrical
System 2450 by Conmed Corporation — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-20653405058158 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
- EUDAMED SRN
- US-MF-000012663
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (6)
- EUDAMED 6f66a72b-8748-4d6c-8937-d8f082115e94 61 fields · synced Jul 18, 2026
- EUDAMED 9f71e8b0-6d27-4470-931c-17faafc79b74 61 fields · synced May 17, 2026
- FDA UDI 3b158c35-6ee6-4cdf-b523-cc62c540a4f0 36 fields · synced May 30, 2026
- FDA UDI 60e68881-faad-46d2-8322-ecd71ef4108c 36 fields · synced May 30, 2026
- EUDAMED d2cb1bb9-0beb-47c9-8d28-4161dae092ff 61 fields · synced Jul 11, 2026
- EUDAMED 14a87bc4-a8aa-40d3-8319-e380ebe25892 61 fields · synced Jul 18, 2026